A closely spaced, serial, light and electron microscopic technique has permitted determination of the patterns of distribution, three dimensional cytoarchitecture and ultrastructural characteristics of developing muscle spindles in the fetal mouse extensor digitorum longus muscle (Figs. 1-6).Spindle development begins at 15 days in utero, when unmyelinated afferent nerves contact large, primary myotubes, located at the muscle's neurovascular hilum. By 17 days in utero the adult number of spindles containing one or two myotubes, can be identified in serial ultrathin sections through the myotube's sensory innervated region. While the primitive capsule of the spindle surrounds the intrafusal myotubes, it is initially confined to the sensory area and does not extend the length of the myotube. At this stage the peripheral regions of the intrafusal myotubes are morphologically indistinguishable from neighboring extrafusal myotubes.It is in this peripheral region that fusimotor innervation will develop.By following the spindles in serial, spaced (i.e., 15μm intervals), ultrathin transverse sections along their length, it is possible to establish the continuity of the sensory innervated region with the peripheral regions of the intrafusal myotube and to determine that fusimotor innervation is not present at 17 days in utero.